Zeigt Titel in Menschen mit Behinderung

Ausgezeichnet mit dem Leipziger Lesekompass 2023. Superheldin mit Hörgerät. ÄTT MÄN ONA UBA MÄN? Das ist alles was Cece versteht, wenn sich die Nachbarjungen über Superhelden unterhalten. Schon als kleines Kind hat Cece ihr Gehör verloren. Seitdem trägt sie ein Hörgerät und hat gelernt, Worte und Sätze von den Lippen abzusehen. Aber Cece hasst das Hörgerät. Es ist riesig und Cece ist sich sicher, dass jeder sie deswegen anstarrt. Bis sie herausfindet, was das Phonic Ear noch alles kann. Denn als "El Taubinio" ist Cece damit selbst schon fast eine Superheldin.

The moving true story of Linda Crosby, an accident survivor who was left permanently and totally disabled, and Roy Crosby, her devoted husband and caregiver, The Day My Life Changed: An Accident Survivor offers a glimpse into the lives of an everyday couple whose love endured and thrived, even in the most impossible odds.

This memoir was written to honor my youngest brother’s influence over my life—the good, the bad, and the ugly, of living with a Down Syndrome sibling. It tells the story of the children of my family, despite our parents’ frailties, remaining committed to each other through life’s many changes and separations. Who I am today is directly related to who I needed to become.

Born 10 weeks premature and given only a 10 percent chance of survival, Rene entered the world fighting for her life. Diagnosed with cerebral palsy, she grew up navigating a society that often defined her by limitations rather than potential. But this audiobook tells a different story—one of determination, courage, humor, and an unshakable belief in the power of being heard.

Hilda’s family didn’t know she had muscular dystrophy. They just knew their preschooler was losing her ability to walk. But they were determined to find a cure. Being disabled in Cameroon meant not only obstacles to transport, but visits to diviners and evangelists, threats of sexual assault, discrimination, and a crisis of faith. Despite the hardship Hilda has faced, her family’s unwavering support and God’s unwavering grace have helped her persevere to become a national broadcaster.

Cory Smit never had a chance to grow up as a normal kid. Between the extreme views pushed on him in church to being bullied at a series of schools, it took years to understand the worst of his trouble at home. After surviving physical and psychological trauma at the hands of his adoptive parents, Cory entered custody of the State of Arizona through a series of misunderstandings and misguided interventions.

From the disability rights advocate and creator of the #DisabledAndCute viral campaign, a thoughtful, inspiring, and charming collection of essays exploring what it means to be black and disabled in a mostly able-bodied white America. Keah Brown loves herself, but that hadn’t always been the...

Having grown up on their great-grandfather’s stories, Royd Tolkien and his brother, Mike, have always enjoyed adventures. So when Mike is diagnosed with motor neurone disease, also known as ALS, the brothers decide to use the time they have left to tick off as much as possible from Mike’s bucket list, from remote camping in Norway to travelling through Royd’s beloved New Zealand. Yet, when Royd loses Mike, he discovers his brother had been writing another kind of bucket list: 50 things he wanted Royd to do after his death.

Mit drei Jahren erlitt Ingrid Mundschin-Bohn eine Hirnhautentzündung, an der sie fast gestorben wäre. In Deutschland, wo sie als Tochter eines deutschen Vaters und einer Schweizer Mutter aufwuchs, war gerade der Krieg zu Ende gegangen, die Medikamente waren immer noch knapp, und die Ärzte wollten keine Antibiotika verschwenden an einem Kind, das in ihren Augen bereits abgeschrieben war. Aber Ingrid Mundschin ließ sich nicht abschreiben, sondern wuchs zu einer lebensfrohen und selbstbewussten Frau heran.

In this fascinating historical adventure, broadcaster and author Selina Mills takes us on a journey through the history of blindness in Western Culture to discover that blindness is not so dark after all. Inspired by her own experience of losing her sight as she forged a successful journalistic career, Life Unseen takes us through a personal and unsentimental historical quest through the lives, stories and achievements of blind people—as well as those sighted people who sought to patronize, demonize and fix them.

As a neurodivergent child in a hundred-year-old house, Zaji Cox collects grammar books, second-hand toys, and sightings of feral cats. She dances and cartwheels through self-discovery and doubt, guided by her big sister and their devoted single mother. Through short essays that evoke the abundant imagination of childhood, Plums for Months explores the challenges of growing up mixed race and low-income on the outskirts of Portland, Oregon.

Mothering under normal circumstances takes all you have to give. But what happens when your child is disabled, and sacrificing all you've got and more is the only hope for a decent future? Full of rage and resilience, duty and love, Ashley Bristowe delivers a mother's voice like no other we've...

Clem Bastow grew up feeling like she’d missed a key memo on human behaviour. She found the unspoken rules of social engagement confusing, arbitrary and often stressful. Friendships were hard, relationships harder and the office was a fluorescent-lit nightmare of anxiety. It wasn’t until Clem was diagnosed as autistic, at age 36, that things clicked into focus. Clem reflects as an autistic adult on her formative experiences as an undiagnosed young person, from the asphalt playground of St Joseph's Primary School in Melbourne to working as an entertainment journalist in Hollywood.

Imagine if you were to lose your sight? Would it feel like the end of everything worthwhile? There is a way forward. Once you realise that blindness is a word and not a sentence, life takes on a new perspective. There are ways to thrive with vision loss. This book reveals how to turn such a life-challenge into a lifestyle you can fully manage and enjoy.

James Partridge was 18 years old in 1977 when his face and body were severely burned in a car accident. Refusing to succumb to society's expectations, James chose not to hide in the shadows, but to succeed despite his distinctive face and live a happy and hugely successful life, both personally and professionally. Face It tells the story of James' recovery and the work he has done ever since to support others with physical differences to cope with the isolation and discrimination they so often face.

Audie Award Finalist for best inspirational book! IMAGE AWARD (Native Daughters of the Golden West) "The Mission Walker is a marvelous book, a moving meditation on the relationships between courage and faith, endurance and transcendence." Randall Sullivan, Creator, The Miracle Detective, Oprah...

Trente-deux ans, c'est le nombre d'années qu'il m'a fallu pour mettre un nom sur ma différence. Comment ai-je pu "passer au travers des mailles du filet" durant tout ce temps ? Je vous révèle, au travers de ce récit parsemé d'anecdotes, comment j'ai grandi dans l'ignorance de mon syndrome. Plongez dans mon quotidien et découvrez chacune des étapes clés de mon évolution ainsi que les moyens mis en œuvre pour survivre dans ce monde parfois difficile à appréhender.

Growing Up Disabled in Australia is the fifth book in the highly acclaimed, best-selling Growing Up series. It includes interviews with prominent Australians such as Senator Jordon Steele-John and Paralympian Isis Holt.

In I'll Pray for You and Other Outrageous Things Said to Disabled People, Hannah Setzer volunteers to go first and say the things that we all think, but rarely say. Hannah has lived her whole life as a disabled woman and is here to share her story, though don't think for a second that this is inspiration porn. In fact, Hannah's disability is the least interesting thing about her!

Sarah Merriman is just like any other urbane young woman in her twenties... She has a job in a Central London hotel, a boyfriend, commutes to work on the Tube, eats out, goes to films and theatre... This is all the more remarkable (though not to her) because Sarah was born with Down's Syndrome. Her parents having no prior inkling, it came as a huge shock to them that they now had a daughter with a disability. In 1999 her father Andy wrote a frank and moving book, A Minor Adjustment, about the challenge of her early years. Now he continues with this inspirational story.